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Trimethylbenzenes, sulfonation

Chem. Descrip. 50-59.9% Calcium sulfonate in 40-49.9% It. aromatic petrol, naphtha (CAS 64742-95-6), 14.4% 1,2,4-trimethylbenzene, 1-4.9% 1,3,5-trimethylbenzene, 1-4.9% 1,2,3-trimethylbenzene Uses Rheology control agent, thixotrope, pigment antisettling agent for urethanes ai high-solids, solv.-based coatings (alkyd, acrylic, polyester, urethanes), baked and air-dried sterns Properties Bm. si. opaque thixotropic gel mild odor insol. in water sp.gr. 1.09 dens. 9.03 Ib/gal vise. 500,000 cps flash pt. (PMCC) 45 C 60% NVbywt. [Pg.437]

Other examples of the action of chlorosulfonic acid on polyalkylbenzenes include 1-ethyl-2,4,6-trimethylbenzene to give the 3-sulfonic acid 1,2,3,5- and 1,2,4,5-tetraethylbenzenes to give high yields of the 4- and 3-sulfonic acids respectively, also pentaethylbenzene gives the 6-sulfonic acid (89%). ... [Pg.39]

The application of pore-expended sulfonic acid SBA-15 has been demonstrated for the first time by Dacquin et al. (2012). In their smdy, the impact of pore-expended sulfonic functionalized SBA-15 toward palmitic acid in esterification and transesterification of tricaprylin and triolein has been explored. Large-pore SBA-15 was obtained by incorporation of trimethylbenzene (TMB) into Pluronic P123/tetraethyl orthosilicate (TEOS) and been aged for 1—3 days. Results showed pore diameters up to 14 nm were achieved through this method, with pore-expansion conferring >3-fold activity toward Cie FFAs esterification and Cg/Cig transesterification reaction (Dacquin et al., 2012). [Pg.147]


See other pages where Trimethylbenzenes, sulfonation is mentioned: [Pg.372]    [Pg.374]    [Pg.372]    [Pg.374]    [Pg.169]    [Pg.323]    [Pg.283]    [Pg.304]    [Pg.362]    [Pg.437]    [Pg.437]    [Pg.346]    [Pg.296]    [Pg.153]    [Pg.39]   
See also in sourсe #XX -- [ Pg.153 , Pg.162 , Pg.175 ]




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1.2.4- Trimethylbenzene

Trimethylbenzenes

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